Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.21864563C>ACA366961615DNAH11c.11402C>A (p.Pro3801His)
c.11423C>A (p.Pro3808His)
7g.21864563C=CA1693722409DNAH11c.11402C= (p.Pro3801=)
c.11423C= (p.Pro3808=)
7g.21864563C>GCA179977DNAH11c.11402C>G (p.Pro3801Arg)
c.11423C>G (p.Pro3808Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21864563C>TCA366961616DNAH11c.11402C>T (p.Pro3801Leu)
c.11423C>T (p.Pro3808Leu)
gnomAD v4
7g.21864564T>ACA453966351DNAH11c.11403T>A (p.Pro3801=)
c.11424T>A (p.Pro3808=)
7g.21864564T>CCA453966353DNAH11c.11403T>C (p.Pro3801=)
c.11424T>C (p.Pro3808=)
dbSNP
7g.21864564T>GCA453966352DNAH11c.11403T>G (p.Pro3801=)
c.11424T>G (p.Pro3808=)
7g.21864565C>ACA366961617DNAH11c.11404C>A (p.Leu3802Ile)
c.11425C>A (p.Leu3809Ile)
7g.21864565C=CA1693722418DNAH11c.11404C= (p.Leu3802=)
c.11425C= (p.Leu3809=)
7g.21864565C>GCA4182740DNAH11c.11404C>G (p.Leu3802Val)
c.11425C>G (p.Leu3809Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.21864565C>TCA366961618DNAH11c.11404C>T (p.Leu3802Phe)
c.11425C>T (p.Leu3809Phe)
7g.21864566T>ACA366961619DNAH11c.11405T>A (p.Leu3802His)
c.11426T>A (p.Leu3809His)
7g.21864566T>CCA366961620DNAH11c.11405T>C (p.Leu3802Pro)
c.11426T>C (p.Leu3809Pro)
7g.21864566T>GCA366961621DNAH11c.11405T>G (p.Leu3802Arg)
c.11426T>G (p.Leu3809Arg)
7g.21864567T>ACA453966354DNAH11c.11406T>A (p.Leu3802=)
c.11427T>A (p.Leu3809=)
7g.21864567T>CCA453966355DNAH11c.11406T>C (p.Leu3802=)
c.11427T>C (p.Leu3809=)
7g.21864567T>GCA453966356DNAH11c.11406T>G (p.Leu3802=)
c.11427T>G (p.Leu3809=)
7g.21864568G>ACA366961624DNAH11c.11407G>A (p.Glu3803Lys)
c.11428G>A (p.Glu3810Lys)
gnomAD v4
7g.21864568G>CCA366961622DNAH11c.11407G>C (p.Glu3803Gln)
c.11428G>C (p.Glu3810Gln)
gnomAD v4
7g.21864568G>TCA366961623DNAH11c.11407G>T (p.Glu3803Ter)
c.11428G>T (p.Glu3810Ter)
7g.21864569A>CCA366961625DNAH11c.11408A>C (p.Glu3803Ala)
c.11429A>C (p.Glu3810Ala)
7g.21864569A>GCA366961626DNAH11c.11408A>G (p.Glu3803Gly)
c.11429A>G (p.Glu3810Gly)
7g.21864569A>TCA366961627DNAH11c.11408A>T (p.Glu3803Val)
c.11429A>T (p.Glu3810Val)
7g.21864570A>CCA366961628DNAH11c.11409A>C (p.Glu3803Asp)
c.11430A>C (p.Glu3810Asp)
7g.21864570A>GCA453966357DNAH11c.11409A>G (p.Glu3803=)
c.11430A>G (p.Glu3810=)
gnomAD v4
7g.21864570A>TCA366961629DNAH11c.11409A>T (p.Glu3803Asp)
c.11430A>T (p.Glu3810Asp)
7g.21864571T>ACA366961630DNAH11c.11410T>A (p.Leu3804Met)
c.11431T>A (p.Leu3811Met)
7g.21864571T>CCA4182741DNAH11c.11410T>C (p.Leu3804=)
c.11431T>C (p.Leu3811=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.21864571T>GCA366961631DNAH11c.11410T>G (p.Leu3804Val)
c.11431T>G (p.Leu3811Val)
7g.21864571T=CA1693722422DNAH11c.11410T= (p.Leu3804=)
c.11431T= (p.Leu3811=)
7g.21864572T>ACA366961632DNAH11c.11411T>A (p.Leu3804Ter)
c.11432T>A (p.Leu3811Ter)
7g.21864572T>CCA366961633DNAH11c.11411T>C (p.Leu3804Ser)
c.11432T>C (p.Leu3811Ser)
7g.21864572T>GCA366961634DNAH11c.11411T>G (p.Leu3804Trp)
c.11432T>G (p.Leu3811Trp)
7g.21864573G>ACA453966358DNAH11c.11412G>A (p.Leu3804=)
c.11433G>A (p.Leu3811=)
gnomAD v4
7g.21864573G>CCA366961636DNAH11c.11412G>C (p.Leu3804Phe)
c.11433G>C (p.Leu3811Phe)
7g.21864573G>TCA366961635DNAH11c.11412G>T (p.Leu3804Phe)
c.11433G>T (p.Leu3811Phe)
gnomAD v4
7g.21864574G>ACA366961637DNAH11c.11413G>A (p.Asp3805Asn)
c.11434G>A (p.Asp3812Asn)
7g.21864574G>CCA366961638DNAH11c.11413G>C (p.Asp3805His)
c.11434G>C (p.Asp3812His)
7g.21864574G>TCA366961639DNAH11c.11413G>T (p.Asp3805Tyr)
c.11434G>T (p.Asp3812Tyr)
7g.21864575A=CA1693722428DNAH11c.11414A= (p.Asp3805=)
c.11435A= (p.Asp3812=)
7g.21864575A>CCA366961640DNAH11c.11414A>C (p.Asp3805Ala)
c.11435A>C (p.Asp3812Ala)
7g.21864575A>GCA4182742DNAH11c.11414A>G (p.Asp3805Gly)
c.11435A>G (p.Asp3812Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21864575A>TCA366961641DNAH11c.11414A>T (p.Asp3805Val)
c.11435A>T (p.Asp3812Val)
7g.21864576T>ACA366961643DNAH11c.11415T>A (p.Asp3805Glu)
c.11436T>A (p.Asp3812Glu)
7g.21864576T>CCA453966360DNAH11c.11415T>C (p.Asp3805=)
c.11436T>C (p.Asp3812=)
7g.21864576T>GCA366961642DNAH11c.11415T>G (p.Asp3805Glu)
c.11436T>G (p.Asp3812Glu)
7g.21864577T>ACA4182743DNAH11c.11416T>A (p.Phe3806Ile)
c.11437T>A (p.Phe3813Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.21864577T>CCA366961644DNAH11c.11416T>C (p.Phe3806Leu)
c.11437T>C (p.Phe3813Leu)
7g.21864577T>GCA366961645DNAH11c.11416T>G (p.Phe3806Val)
c.11437T>G (p.Phe3813Val)
7g.21864577T=CA1693722433DNAH11c.11416T= (p.Phe3806=)
c.11437T= (p.Phe3813=)

Number of alleles fetched